Canonical Allele Identifier: CA2697267296
Gene: NTRK1 HGNC NCBI

Linked Data

dbSNP Id: rs1393371321

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.156879059C>A , CM000663.2:g.156879059C>A GRCh38
NC_000001.10:g.156848851C>A , CM000663.1:g.156848851C>A GRCh37
NC_000001.9:g.155115475C>A NCBI36
NG_007493.1:g.68310C>A , LRG_261:g.68310C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000674537.2:c.1626-63C>A ENSP00000502725.1:n.1626-63C>A
ENST00000392302.7:c.1626-63C>A ENSP00000376120.3:n.1626-63C>A
ENST00000497019.7:c.*398-63C>A ENSP00000436804.2:n.*398-63C>A
ENST00000524377.7:c.1806-63C>A MANE Select ENSP00000431418.1:n.1806-63C>A
ENST00000674537.1:c.1626-63C>A ENSP00000502725.1:n.1626-63C>A
ENST00000358660.3:c.1797-63C>A ENSP00000351486.3:n.1797-63C>A
ENST00000368196.7:c.1788-63C>A ENSP00000357179.3:n.1788-63C>A
ENST00000392302.6:c.1698-63C>A ENSP00000376120.2:n.1698-63C>A
ENST00000497019.6:c.*398-63C>A ENSP00000436804.1:n.*398-63C>A
ENST00000524377.5:c.1806-63C>A ENSP00000431418.1:n.1806-63C>A
ENST00000530298.5:n.2259-63C>A
NM_001007792.1:c.1698-63C>A , LRG_261t1:c.1698-63C>A NP_001007793.1:n.1698-63C>A
NM_001012331.1:c.1788-63C>A , LRG_261t2:c.1788-63C>A NP_001012331.1:n.1788-63C>A
NM_002529.3:c.1806-63C>A , LRG_261t3:c.1806-63C>A NP_002520.2:n.1806-63C>A
NM_001012331.2:c.1788-63C>A NP_001012331.1:n.1788-63C>A
NM_002529.4:c.1806-63C>A MANE Select NP_002520.2:n.1806-63C>A